Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the ATP13A2 Gene. Issue 7 (12th July 2022)

Record Type:
Journal Article
Title:
Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the ATP13A2 Gene. Issue 7 (12th July 2022)
Main Title:
Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the ATP13A2 Gene
Authors:
Algahtani, Hussein
Shirah, Bader
Alshammari, Salem
Alghamdi, Fareeda
Abdulkareem, Angham Abdulrhman
Naseer, Muhammad Imran
Abstract:
Is Part Of:
Movement disorders clinical practice. Volume 9:Issue 7(2022)
Journal:
Movement disorders clinical practice
Issue:
Volume 9:Issue 7(2022)
Issue Display:
Volume 9, Issue 7 (2022)
Year:
2022
Volume:
9
Issue:
7
Issue Sort Value:
2022-0009-0007-0000
Page Start:
997
Page End:
1002
Publication Date:
2022-07-12
Subjects:
ATP13A2 -- hereditary spastic paraplegia 78 -- autosomal recessive -- mutation -- Saudi Arabia
Movement Disorders
Movement disorders -- Periodicals
Movement disorders
Periodicals
Periodicals
616
Journal URLs:
http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%292330-1619 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:
10.1002/mdc3.13508 ↗
Languages:
English
ISSNs:
2330-1619
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - 5980.317300
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:
24409.xml